Variant report

Variant	rs186169789
Chromosome Location	chr12:121717735-121717736
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:121716004..121718724-chr12:121719656..121721765,2	MCF-7	breast:
2	chr12:121711495..121713766-chr12:121715448..121718429,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000110931	Chromatin interaction

Extended variants
information (count: 9 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
5	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
6	nsv1050519	chr12:121552964-121756420	Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
7	nsv1048801	chr12:121695522-121761800	Flanking Active TSS Strong transcription Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	9 gene(s)	inside rSNPs	diseases
8	esv3426955	chr12:121717642-121719096	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	nsv983372	chr12:121717728-121721054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:119 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121679600-121732600	Strong transcription	Fetal Intestine Small	intestine
2	chr12:121681200-121717800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr12:121688400-121733000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr12:121706600-121726400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:121707000-121733200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
6	chr12:121707400-121720200	Weak transcription	K562	blood
7	chr12:121707400-121733200	Weak transcription	HSMM	muscle
8	chr12:121707600-121719200	Weak transcription	H9 Cell Line	embryonic stem cell
9	chr12:121707600-121724600	Weak transcription	Fetal Brain Male	brain
10	chr12:121708800-121730200	Weak transcription	HepG2	liver
11	chr12:121708800-121733400	Weak transcription	HSMMtube	muscle
12	chr12:121709200-121719000	Weak transcription	HUES64 Cell Line	embryonic stem cell
13	chr12:121709200-121726000	Weak transcription	Primary B cells from peripheral blood	blood
14	chr12:121709400-121718600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr12:121711400-121719800	Weak transcription	Small Intestine	intestine
16	chr12:121711400-121732200	Weak transcription	Hela-S3	cervix
17	chr12:121711800-121732200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
18	chr12:121712000-121725400	Weak transcription	Primary hematopoietic stem cells	blood
19	chr12:121712000-121729000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr12:121712000-121732000	Weak transcription	Primary T cells fromperipheralblood	blood
21	chr12:121712200-121726000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
22	chr12:121712200-121728400	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr12:121712400-121718200	Weak transcription	HUES48 Cell Line	embryonic stem cell
24	chr12:121712400-121719000	Weak transcription	Colon Smooth Muscle	Colon
25	chr12:121712400-121719800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr12:121712400-121721000	Weak transcription	Rectal Mucosa Donor 31	rectum
27	chr12:121712400-121721000	Weak transcription	Dnd41	blood
28	chr12:121712400-121727000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chr12:121712400-121733000	Weak transcription	Rectal Smooth Muscle	rectum
30	chr12:121712400-121733200	Weak transcription	Aorta	Aorta
31	chr12:121712600-121719000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr12:121712600-121720800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
33	chr12:121712600-121726200	Weak transcription	Thymus	Thymus
34	chr12:121712600-121732200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
35	chr12:121713000-121728400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr12:121713000-121732200	Weak transcription	Primary T helper cells fromperipheralblood	blood
37	chr12:121713600-121719200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr12:121714200-121718000	Enhancers	HUVEC	blood vessel
39	chr12:121714600-121719400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr12:121714800-121717800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
41	chr12:121715200-121730200	Weak transcription	A549	lung
42	chr12:121715400-121731400	Weak transcription	Primary T helper cells PMA-I stimulated	--
43	chr12:121715600-121718000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr12:121715600-121722400	Weak transcription	Osteobl	bone
45	chr12:121715600-121723000	Weak transcription	Fetal Kidney	kidney
46	chr12:121715600-121733000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr12:121715600-121733000	Weak transcription	NHEK	skin
48	chr12:121715800-121717800	Strong transcription	Fetal Brain Female	brain
49	chr12:121715800-121718000	Enhancers	Ovary	ovary
50	chr12:121716200-121717800	Enhancers	Right Atrium	heart

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